DR JS NATURAL ADVANCED FORMULA HAND SANITIZER gel

Dr Js Natural Advanced Formula Hand Sanitizer by

Drug Labeling and Warnings

Dr Js Natural Advanced Formula Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by QYK BRANDS LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antimicrobial

Uses

● Hand Sanitizer to help decrease bacteria on the skin that could cause disease. ● Recommended for repeated use.

Warnings

Flammable. Keep away from fire or flame, For external use only.When using this product,do not use in or near the eyes.In case of contact,rinse eyes thoroughly with water.Stop use and ask doctor if irritation or rash appears and lasts,Keep out of reach for children if swallowed,get medical help of contact a Poison Control Center right away.

Do Not Use:

Stop use and ask a doctor if ● Irritation and redness develops. ● Condition persists for more than 72 hours.

When using this product:

● Avoid contact with eyes. In case of contact with eyes, flush thoroughly with water. ● Avoid contact with broken skin. ● Do not inhale or ingest.

Stop:

Stop use and ask a doctor if ● Irritation and redness develops. ● Condition persists for more than 72 hours.

Childeren Safety

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions ● Pump as needed into your palms and thoroughly spread on both hands. Rub into skin until dry. ● For children under 6, use only under adult supervision. ● Not recommended for infants.

Other information

Store below 110°(43°C)

May discolor certain fabrics or surfaces

Inactive ingredients

Inactive ingredients Water, Glycerin, Aloe vera, Carbomer, Polyacrylate crosspolymer, Fragrance

PRINCIPAL DISPLAY PANEL

NDC

INGREDIENTS AND APPEARANCE

DR JS NATURAL ADVANCED FORMULA HAND SANITIZER 
dr js natural advanced formula hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73750-369
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73750-369-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020
2	NDC: 73750-369-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020
3	NDC: 73750-369-03	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020
4	NDC: 73750-369-04	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020
5	NDC: 73750-369-05	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020
6	NDC: 73750-369-06	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020
7	NDC: 73750-369-07	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/31/2020

Labeler - QYK BRANDS LLC (081560441)

Registrant - QYK BRANDS LLC (081560441)

Establishment
Name	Address	ID/FEI	Business Operations
QYK BRANDS LLC		081560441	manufacture(73750-369)